Cobilinschi Cristian, Mirea Liliana, Andrei Cosmin-Andrei, Ungureanu Raluca, Cotae Ana-Maria, Avram Oana, Isac Sebastian, Grințescu Ioana Marina, Țincu Radu
Department of Anesthesiology and Intensive Care II, Carol Davila University of Medicine, and Pharmacy, 050474 Bucharest, Romania.
Department of Anesthesiology and Intensive Care, Clinical Emergency Hospital Bucharest, 014461 Bucharest, Romania.
Toxics. 2023 Nov 9;11(11):917. doi: 10.3390/toxics11110917.
The administration of intravenous lipid emulsion (ILE) is a proven antidote used to reverse local anesthetic-related systemic toxicity. Although the capacity of ILE to generate blood tissue partitioning of lipophilic drugs has been previously demonstrated, a clear recommendation for its use as an antidote for other lipophilic drugs is still under debate. Venlafaxine (an antidepressant acting as a serotonin-norepinephrine reuptake inhibitor (SNRI)) and quetiapine (a second-generation atypical antipsychotic) are widely used in the treatment of psychotic disorders. Both are lipophilic drugs known to induce cardiotoxicity and central nervous depression. We report the case of a 33-year-old man with a medical history of schizoaffective disorder who was admitted to the emergency department (ED) after having been found unconscious due to a voluntary ingestion of 12 g of quetiapine and 4.5 g of venlafaxine. Initial assessment revealed a cardiorespiratory stable patient but unresponsive with a GCS of 4 (M2 E1 V1). In the ED, he was intubated, and gastric lavage was performed. Immediately after the admission to the intensive care unit (ICU), his condition quickly deteriorated, developing cardiovascular collapse refractory to crystalloids and vasopressor infusion. Junctional bradycardia occurred, followed by spontaneous conversion to sinus rhythm. Subsequently, frequent ventricular extrasystoles, as well as patterns of bigeminy, trigeminy, and even episodes of non-sustained ventricular tachycardia, occurred. Additionally, generalized tonic-clonic seizures were observed. Alongside supportive therapy, antiarrhythmic and anticonvulsant therapy, intravenous lipid emulsion bolus, and continuous infusion were administered. His condition progressively improved over the following hours, and 24 h later, he was tapered off the vasopressor. On day 2, the patient repeated the cardiovascular collapse and a second dose of ILE was administered. Over the next few days, the patient's clinical condition improved, and he was successfully weaned off ventilator and vasopressor support. ILE has the potential to become a form of rescue therapy in cases of severe lipophilic drug poisoning and should be considered a viable treatment for severe cardiovascular instability that is refractory to supportive therapy.
静脉输注脂质乳剂(ILE)是一种已被证实的解毒剂,用于逆转局部麻醉药相关的全身毒性。尽管此前已证明ILE能够使亲脂性药物在血液与组织间形成分配,但对于将其用作其他亲脂性药物的解毒剂仍存在争议。文拉法辛(一种作为5-羟色胺-去甲肾上腺素再摄取抑制剂(SNRI)的抗抑郁药)和喹硫平(一种第二代非典型抗精神病药)广泛用于治疗精神障碍。二者均为亲脂性药物,已知可诱发心脏毒性和中枢神经抑制。我们报告了一名33岁患有分裂情感性障碍病史的男性病例,他因自愿服用12克喹硫平和4.5克文拉法辛后被发现昏迷而被收入急诊科(ED)。初始评估显示该患者心肺功能稳定,但无反应,格拉斯哥昏迷评分(GCS)为4分(运动2分、睁眼1分、言语1分)。在急诊科,他接受了气管插管并进行了洗胃。在被收入重症监护病房(ICU)后,他的病情迅速恶化,出现了对晶体液和血管升压药输注无反应的心血管衰竭。出现交界性心动过缓,随后自发转为窦性心律。随后,频繁出现室性早搏,以及二联律、三联律模式,甚至非持续性室性心动过速发作。此外,还观察到全身性强直阵挛发作。除了支持治疗、抗心律失常和抗惊厥治疗外,还给予了静脉脂质乳剂推注和持续输注。在接下来的几个小时里,他的病情逐渐好转,24小时后,逐渐停用血管升压药。在第2天,患者再次出现心血管衰竭,于是给予了第二剂ILE。在接下来的几天里,患者的临床状况有所改善,并成功撤掉了呼吸机和血管升压药支持。ILE有可能成为严重亲脂性药物中毒病例的一种抢救治疗方式,对于对支持治疗无反应的严重心血管不稳定情况,应考虑将其作为一种可行的治疗方法。